Article
Neurodevelopmental outcome in 22q11.2 deletion syndrome and management.
American journal of medical genetics. Part A - 1 Oct 2018
Swillen Ann, Moss Edward, Duijff Sasja
Abstract excerpt
The 22q11.2 deletion syndrome (22q11.2 DS) places affected individuals at an increased risk for neurodevelopmental/cognitive, behavioral and social-emotional difficulties. Poor cognitive functioning and intellectual disabilities, attention and executive functioning deficits, learning disorders, emotional dysregulation and impairments in social processing are common among individuals with 22q11.2 DS. Identifying...
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